Methylenetetrahydrofolate reductase homozygous mutation in a young boy with cerebellar infarction

Posterior circulation vascular occlusive disease in children is a rare and uncommonly reported event. Among the numerous risk factors, the methylenetetrahydrofolate reductase (MTHFR) mutation is considered to be a common genetic cause of thrombosis in adults and children. Recently, a link between th...

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Detalhes bibliográficos
Main Authors: Spalice, Alberto, Del Balzo, Francesca, Perla, Francesco Massimo, Properzi, Enrico, Carducci, Carla, Antonozzi, Italo, Iannetti, Paola
Formato: Artigo
Idioma:Inglês
Publicado em: PAGEPress Publications 2009
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3096031/
https://ncbi.nlm.nih.gov/pubmed/21589820
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4081/pr.2009.e4
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